A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033862



Internal ID19123083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17601432..17738758hg38UCSC Ensembl
Innerchr5:17601541..17738867hg19UCSC Ensembl
Innerchr5:17644644..17774596hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38137327
hg19137327
hg18129953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5588n100
Supporting Variantsnssv3635827
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033862
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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